Evidence map›Paper›PMID 37452848›Full record

ArticleJournal of cancer research and clinical oncology2023

Dynamic changes in three biomarkers predict early-stage hepatocellular carcinoma in patients with chronic hepatitis B receiving antiviral therapy.

Qianyu Zhu, Jialing Zhou, Hongyi Li, Hui Wang, Jiangbo Ren, Shujie Sun, Miaoran Yang, Shanshan Wu, Ming Cao, Kaixiang Wang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Qianyu Zhu *Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Jialing Zhou *Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Hongyi LiLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Hui WangLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Jiangbo RenLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Shujie SunLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Miaoran YangLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Shanshan WuNational Clinical Research Center for Digestive Diseases, Beijing, China.
Ming CaoMolecular Biology Laboratory, Baoding People's Hospital, Baoding, China.
Kaixiang WangMolecular Biology Laboratory, Baoding People's Hospital, Baoding, China.
Hong YouLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China. youhong30@sina.com.
Hong MaLiver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China. mahongmd@163.com.
Beijing Friendship Hospital · CNCapital Medical University · CNBaoding People's Hospital · CNNational Clinical Research Center for Digestive Diseases · CN

Funding

National Science and Technology Major Project 2013ZX10002004National Science and Technology Major Project 2017ZX10202202
6 · The paper itself

Abstract

purposePatients with chronic hepatitis B (CHB) remain at risk for hepatocellular carcinoma during antiviral therapy. We aimed to clarify the values of alpha-fetoprotein (AFP), lectin-reactive fraction of AFP (AFP-L3), and des-γ-carboxyprothrombin (DCP) for early warning of HCC.

methodsA total of 1348 CHB patients received antiviral therapy and follow-up every 26 weeks. Eighty-four patients with HCC were age-, sex-, and cirrhosis-matched with 168 controls. AFP, AFP-L3, and DCP were compared between the groups from 104 weeks before HCC diagnosis (- 104 w) to the time of diagnosis (0 w).

resultsOf the 84 HCC patients, 60 (71.4%) had early-stage HCC, AFP increased from - 26 w, and AFP-L3 and DCP increased from - 78 w. However, levels were unchanged in controls. ΔAFP, ΔAFP-L3, and ΔDCP showed similar abilities for predicting HCC (P > 0.05). Receiver operating characteristic curve analysis showed that AFP had better diagnostic performance for HCC than AFP-L3, DCP, or their combination. The cut-off values of AFP, AFP-L3, and DCP were 5.3 ng/mL, 1.05%, and 31.5 mAU/mL, respectively. Notably, lower AFP values were required to diagnose HCC in patients with detectable HBV DNA (4.1 ng/mL) or elevated alanine aminotransferase (5.2 ng/mL).

conclusionsChanges in AFP, AFP-L3, and DCP can help to predict HCC in CHB patients receiving antiviral therapy. A lower AFP value is needed to diagnose HCC, especially in patients with detectable HBV DNA or elevated alanine aminotransferase.

Indexed as

Antiviral agentBiomarkerDiagnosisHepatocellular carcinomaLiver cirrhosis

Identifiers

PMID37452848
PMCPMC11797701
OpenAlexW4384406450

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.